Always ex-KAI-ted to see him

In my previous post I told you briefly about my other baby Kai. He is the most beautiful boy and he has a special place in our family. Mind you I’m super in love with this boy, super duper!

Kai has NKH (non ketotic hyperglycinemia), it is extremely rare and only affects 1 child in every 60,000 born. Nkh is caused by a defect in the genetic code machinery, so in short children with this disorder cannot break down the amino acid glycine. As we were taught in our science class in school amino acids are natural components of our baby. So since glycine is not broken down it then accumulates in the body,and glycine is a super important molecule in the brain  where it has various functions such as transmitting signals from one cell to another (brain cell). So since there is a build up of glycine, it disrupts the function of the brain.

Kai is a very special boy, he is very handsome, cheeky (as he takes his socks all the time), he makes those very cute noises that makes you say aah how adorable he is, he has the most ridiculous cheeks they are so cute if only I can bite and squeeze them! (I’m sorry Kai, I can’t help it), he has the most beautiful smile ever, his smile is heart melting.

If you have a spare change, if you can donate just a small amount,  if you can fundraise,  every little thing helps. So what if you don’t know them, so what if you haven’t met them, we can help and we can make a difference. It’s not a waste of help, it goes somewhere and that money we raise and donate goes to funding a cure for nkh.

These beautiful children deserves a bright future, and their future is in the horizon. Please donate and help us raise money to find a cure, think how beautiful Kai is and think the life he deserves, nobody deserves nkh, nobody deserves to suffer, not Kai, not anybody else.

http://www.teammikaere.com
http://fundnkhcure.com